Lead Quality Assurance Software Developer

• Develop and implement UAT test strategies, plans, and test cases for the Majesco platform. • Collaborate with business users, business analysts, and development teams to understand requirements and define test scope. • Lead the UAT Test team in executing business test cases and verify results with business sponsors and business team. • Ensure all test cases are executed, and defects are logged, tracked, and resolved in a timely manner. • Conduct risk assessments and prioritize testing efforts based on project timelines and requirements. • Identify opportunities for test automation and drive the implementation of automation frameworks. • Continuously improve testing processes, tools, and methodologies to enhance efficiency and effectiveness. • Ensure that the automation scripts are maintained and updated regularly. • Lead and mentor a team of QA engineers, providing guidance, training, and support. • Allocate tasks and resources effectively to ensure project deadlines are met. • Work closely with cross-functional teams to ensure alignment on quality goals. • Communicate test results, progress, risks, and issues to stakeholders effectively. • Participate in Agile ceremonies such as sprint planning, daily stand-ups, and retrospectives. • Leverage deep knowledge of the Majesco platform to ensure test coverage and quality. • Provide subject matter expertise on Majesco-specific testing challenges and best practices. • Stay updated with the latest Majesco product updates and releases to ensure alignment with testing activities. • 6 to 9 years of experience in QA, with at least 3 years of experience working with the Majesco platform. • Proven experience in leading QA and UAT teams and managing testing projects from start to finish. • Strong knowledge of QA methodologies, tools, and processes. • Experience with test automation tools (e.g., Selenium, UFT, JUnit) and frameworks. • Proficient in writing SQL queries for database validation. • Familiarity with API testing tools like Postman, SoapUI, or RestAssured. • In-depth understanding of the insurance domain, particularly property and casualty (P&C) insurance. • Experience with Majesco\'s core insurance platform, including policy, billing, and claims modules. • Excellent leadership and team management skills. • Strong analytical and problem-solving abilities. • Effective communication and interpersonal skills. • Ability to work in a fast-paced, Agile environment. Optional to help sourcing calibration

Join Our Asthma Study: Get Free Treatment, Compensation, and a $100 Referral Bonus! We are seeking volunteers for a clinical trial to test the effectiveness of a new medication for treating Severe Asthma linked to high Eosinophil levels. The study aims to evaluate if this treatment can help control Asthma symptoms and achieve clinical remission. Participation is free of charge, and you will be compensated for your time and travel. Additionally, if you refer a friend who qualifies, you can earn a bonus of $100. We are seeking volunteers for a clinical study evaluating the safety and effectiveness of a treatment for Severe Eosinophilic Asthma. If you or someone you know may be interested, please contact us to learn more about eligibility and potential benefits. Call 626-822-6554 Now! Or Apply Here Why Participate? ● Compensation: Get compensated up to $100 per clinic visit with no cost to you or your insurance! ● Comprehensive Support: Regular check-ins and assessments to ensure your health is a priority. Our trial is conducted by experienced healthcare professionals dedicated to your well-being. ● No-cost study medications: Study medication for Severe Eosinophilic Asthma is given at no cost! To qualify: ● Be at least 18 years of age or older ● Clinically diagnosed with Asthma by a physician ● Haven't used NUCALA (Mepolizumab) in the last 6 months Check out our other studies! ● Foot Ulcers ● Vitiligo ● Future Studies Pasadena Clinical Trials Your participation can help advance research and improve lives. If you're ready to take action, contact us at 626-822-6554 or visit the Pasadena Clinical Trials website for more information. Get Involved Today!

Experience: 5 Years Duties and Responsibilities As a Web Accessibility Specialist, you will lead all testing and audit activities using manual and automated accessibility testing tools and assistive technologies. Conduct accessibility testing using a combination of automated tools and manual testing (including testing with assistive technologies) to evaluate the level of conformance to the Web Content Accessibility Guidelines (WCAG) and other applicable standards and regulatory requirements. Create, document, and manage test plans, testcases, and scripts across multiple projects based on software requirements and design documents. Conduct functional, end-to-end, and regression testing of applications to ensure functionality, reliability, and quality. Create and maintain test scripts, standards, guidelines, and playbooks for accessibility testing and development best practices. Document and report defects, issues, and areas of improvement as well as manage and prioritize critical ADA defects. Collaborate with Business Analysts and Clients to understand requirements and provide feedback. Act as a subject matter expert for testing web and mobile applications for accessibility. Participate in system designs, Support, and foster usability testing and research for accessibility. Provide ad-hoc, project-based team training for ADA awareness, implement solutions, and foster innovation through accessibility. Preferred Qualifications: ·Bachelor’s degree in computer science, IT, MIS,Engineering, or related fields. ·7+ years of experience as a Quality Analyst withdemonstrated knowledge of quality assurance methodology and practices. ·        Hands-on experience with automated test tools and test management tools like Jira or GitLab. ·        In-depth, working knowledge of ADA tools and standards for accessibility testing (i.e., WAVE, JAWS, axe, ANDI, and other automated tools or applications). ·        5+ years of experience in User Acceptance Testing (UAT) methodologies to ensure digital products adhere to enterprise conformance levels (WCAG 2.0, 2.1 level AA) within agile projects. ·        Ability to provide solutions for testers and development teams by applying best practices. Ability to provide direction and lead QA testers. ·        Ability to effectively utilize assistive technologies such as JAWS, NVDA, Voiceover, TalkBack, and other manual and automated testing tools across multiple devices, browsers, and operating systems. ·        Certified Professional in Web Accessibility (CPWA) or Web Accessibility Specialist (WAS) certification. ·        Working knowledge of HTML5 and CSS.

Join Our Asthma Study: Get Free Treatment, Compensation, and a $100 Referral Bonus! We are seeking volunteers for a clinical trial to test the effectiveness of a new medication for treating Severe Asthma linked to high Eosinophil levels. The study aims to evaluate if this treatment can help control Asthma symptoms and achieve clinical remission. Participation is free of charge, and you will be compensated for your time and travel. Additionally, if you refer a friend who qualifies, you can earn a bonus of $100. We are seeking volunteers for a clinical study evaluating the safety and effectiveness of a treatment for Severe Eosinophilic Asthma. If you or someone you know may be interested, please contact us to learn more about eligibility and potential benefits. Call 626-822-6554 Now! Or Apply Here Why Participate? ● Compensation: Get compensated up to $100 per clinic visit with no cost to you or your insurance! ● Comprehensive Support: Regular check-ins and assessments to ensure your health is a priority. Our trial is conducted by experienced healthcare professionals dedicated to your well-being. ● No-cost study medications: Study medication for Severe Eosinophilic Asthma is given at no cost! To qualify: ● Be at least 18 years of age or older ● Clinically diagnosed with Asthma by a physician ● Haven't used NUCALA (Mepolizumab) in the last 6 months Check out our other studies! ● Foot Ulcers ● Vitiligo ● Future Studies Pasadena Clinical Trials Your participation can help advance research and improve lives. If you're ready to take action, contact us at 626-822-6554 or visit the Pasadena Clinical Trials website for more information. Get Involved Today!

Continental Disc Corporation, LLC (“CDC”) designs and manufactures safety-critical products that protect pressure-containing vessels from catastrophic failure. CDC is headquartered in Liberty, Missouri (outside Kansas City), and has manufacturing operations in Houston, Texas, and Ahmedabad, India with additional sales offices in India, the Netherlands and China. CDC benefits from one of the most recognized brands in its industry and a reputation for outstanding quality earned over its 60 years of operation. CDC’s customers include blue-chip companies in the chemicals, oil and gas, pharmaceutical, general industrial, aerospace, defense, food and beverage, municipal, and other markets globally. Under the supervision of Quality Assurance Manager - Disc this position is responsible for assisting in defining, implementing, and maintaining all aspects of the quality management system (QMS) practices and procedures, as well as PED, ATEX, and NQA-1 certifications.  This position will work closely with the site QA Manager to ensure that the processes and procedures within the QMS are adhered to by site personnel as well as ensure that these associated business processes are aligned. This role, in conjunction with the site QA Manager, will be responsible for the execution of the site level internal audits and managing external audits. In addition, the QA Engineering will assist the QA Manager in the analysis of discrepancies in performance measures and compliance and will initiate actions with the site level managers to ensure compliance with those measures.    Requirements - Develop and implement quality systems, manuals and procedures to comply with AS9100/ISO9001, PED, ATEX, NQA-1, customer and other regulatory requirements. - Performs internal audits and reports to management on the effectiveness of the QMS and suggestions for improvement. - Perform system audits of other company facilities and suppliers. - Represents Company in regulatory and customer audits, facility surveys and third-party inspections. - Work to facilitate corrective actions to resolve nonconformities, especially related to system and standard compliance and product conformity. - Assist and advise the QA Manager and Quality Supervisor on issues related to compliance as needed.  - Ensure compliance with regulatory agencies, documented procedures, engineering specifications, and customer requirements. - Provide training programs and instruction to employees related to regulatory and statutory compliance. - Work to maintain and develop QMS documentation (procedures, manuals, etc.) which meet all statutory and regulatory requirements. - Assists in Contract Review and Project reviews to identify all requirements and perform analysis on CDC’s ability to meet those requirements. - Works in conjunction with the QC supervisor to assist and answer questions that arise from QC inspectors. - Coordinate problem solving teams to identify and implement improvement activities. - Perform other duties as assigned, based on workload and business need. EDUCATION AND EXPERIENCE: - Bachelor's degree or equivalent with three (3) years’ experience in quality assurance in a manufacturing environment.  - Knowledge of manufacturing processes such as welding, metallurgy, testing of rupture discs/valves, and process control techniques. - Experience in the maintenance of QMS. - Experience as an Internal Auditor for standards such as ISO9001, AS9100, IATF16949, NQA-1 - Experience in working with suppliers and supply chain to resolve issues. - Experience in leading and facilitating RCCA’s. TECHNICAL / FUNCTION SPECIFIC: - Strong computer skills sufficient to successfully use company ERP system, MS Office, and statistical methods - Working knowledge of process improvement methodology and application (e.g., Lean, Six Sigma, Quality Principles) - Math and calculation - Problem solving and RCCA - Data gathering and analysis - Critical thinking, reasoning and analyzing - Detailed understanding of quality management systems (ISO, AS, APEX, etc). - Effective verbal and written communication and presentation skills - Well-developed planning and organizational skills - Knowledge of applicable certification standards and codes BEHAVORIAL: - Is good at establishing clear directions; sets stretching objectives; distributes the workload appropriately; lays out work in a well-planned and organized manner; maintains two-way dialogue with others on work and results; brings out the best in people; is a clear communicator. - Attention to detail. - Makes good decisions based upon a mixture of analysis, wisdom, experience, and judgement; most solutions and suggestions turn out to be correct and accurate when judged over time; sought out by others for advice and solutions. - Can quickly find common ground and solve problems for the good of all; can represent own interests and yet be fair to other groups; can solve problems with peers with a minimum of noise; is seen as a team player and is cooperative; easily gains trust and support of peers; encourages collaboration; can be candid with peers. - Uses time effectively and efficiently; values time; concentrates efforts on the more important priorities; gets more done in less them than others; can attend to a broader range of activities. - Has the functional and technical knowledge and skills to do the job at a high level of accomplishment. - Good at figuring out the processes necessary to get things done; knows how to organize activities; understands how to separate and combine tasks into efficient workflow; knows what to measure and how to measure it; can see opportunities for synergy and integration where others can’t; can simplify complex process; gets more out of fewer resources. - Can be counted on to exceed goals successfully; bottom-line oriented; steadfastly pushes self and others for results. - Sincere dedication to the best interests of the company, its customers and employees. - Create a climate in which people want to do their best; can motivate many kinds of direct reports and team; can assess each person’s not button and use it to get the best out from them; pushes tasks and decisions down; empowers others; invites input from each person and shares ownership and visibility; makes each individual feel their work is important; is someone people like working for and with. - Provides challenging and stretching tasks and assignments; holds frequent development discussions; is aware of each person’s career goals; constructs compelling development plans and executes them; pushes people to accept developmental moves; will take on those who need help and further development; cooperates with the developmental system in the organization; is a people builder - Concern for quality, accuracy, and safety. PHYSICAL REQUIREMENTS: - Sufficient manual dexterity to successfully use a computer. - Ability to sit for extended periods of time, up to 8 hours per day, though possibly more when overtime is required. - Frequently required to stand and/or walk, up to 2 hours per day, and make frequent trips from the office area to the manufacturing area. - Ability to wear all required personal protective equipment when in the manufacturing area, including, but not limited to, safety glasses and safety shoes. - Minor travel may be required (Benefits Medical, Dental, Vision, FSA and 401K with Match eligible day one. Employee Assistance Program, Short Term Disability, Long Term Disability, Basic Life, Voluntary Life, Voluntary Accident, Voluntary Hospital Indemnity, Voluntary Cancer Plan, Fitness Room, Safety Shoe Reimbursement, Prescription Eye Glass Allowance, 12 Holidays* (one floating) , Paid time off, Tuition Reimbursement and so much more. Equal Opportunity Employer As an Equal Opportunity Employer, CDC does not discriminate in its employment decisions on the basis of race, religion, color, national origin, sex orientation, gender identity, pregnancy, familial status, age, disability, veteran or military status, genetic information, or any other basis that would be in violation of any applicable federal, state, or local law. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

Research Study for Volunteers The California Clinical Trials Medical Group managed by Parexel, located in Glendale, CA is currently seeking volunteers to aid in the development of an active database of participants for metabolic conditions. We are recruiting the following populations: • Male and Females • Ages 18 or older • BMI 27 and up The study involves: • 1 screening visit As compensation for your time and participation, you may receive up to $100 For more information, please contact us toll free at 1-888-CC-TRIAL or 1-888-228-7425 (Monday to Friday between 8AM and 4PM). Please reference study # 289937